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Involvement of metabotropic glutamate receptor 5 in the inhibition of methamphetamine-associated contextual memory after prolonged extinction training

机译:长时间灭绝训练后,代谢型谷氨酸受体5参与抑制甲基苯丙胺相关的背景记忆

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Addiction is thought to be a memory process between perception and environmental cues and addicted patients often relapse when they come into contact with the drug-related context once again. Here, we used a conditioned place preference protocol to seek a more effective extinction methodology of methamphetamine (METH) memory and delineate its underlying mechanism. Conditioning METH for 3days in mice markedly increased the time spent in the METH-paired compartment. Then the mice were conditioned with saline for 6days, from day 6 to day 11, a procedure termed extinction training. However, METH memory returned after a priming injection of METH. We prolonged extinction duration from 6 to 10days and found that this extensive extinction (EE) training prevented priming effect. At the molecular level, we discovered that prolonged extinction training reversed the METH-conditioned place preference-induced increase in surface expression of GluA2 and alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate (AMPA)/NMDA ratio in the basolateral amygdala. In addition, we found that extinction with metabotropic glutamate receptor 5 (mGluR5) activation had similar results to EE: reduced relapse after extinction, decreased synaptic AMPA receptors AMPARs and the AMPA/NMDA ratio. On the contrary, EE with mGluR5 inhibition suppressed the results of EE. These data indicate that EE training-elicited inhibition of METH-primed reinstatement is mediated by the mGluR5.
机译:成瘾被认为是感知和环境暗示之间的记忆过程,成瘾的患者在再次与毒品有关的情况下经常会复发。在这里,我们使用条件位置偏爱协议来寻求更有效的甲基苯丙胺(METH)记忆灭绝方法,并描述其潜在机制。在小鼠中将METH调理3天,可明显增加在METH配对室中所花费的时间。然后,从第6天到第11天,用盐水使小鼠适应6天,该过程称为灭绝训练。但是,初次注入METH后,METH记忆恢复了。我们将灭绝时间从6天延长到10天,发现这种广泛的灭绝(EE)训练阻止了启动效应。在分子水平上,我们发现长时间的灭绝训练可以逆转METH条件的位置优先诱导的GluA2和α-氨基-3-羟基-5-甲基异恶唑-4-丙酸酯(AMPA)/ NMDA的表面表达的表面表达增加。基底外侧杏仁核。此外,我们发现具有代谢型谷氨酸受体5(mGluR5)活化的灭绝与EE相似:灭绝后复发减少,突触AMPA受体AMPAR和AMPA / NMDA比降低。相反,具有mGluR5抑制作用的EE抑制了EE的结果。这些数据表明,mGluR5介导了EE训练引起的对METH启动的恢复的抑制。

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